Computerized System Validation jobs in MO

Wilson, North Carolina

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Today

We are looking for a Validation Engineer for our client in Wilson, NC Job Title: Validation Engineer Job Location: Wilson, NC Job Type: Contract Job Description: Responsibilities: Participate in the commissioning, qualification and start-up of various pharmaceutical cGMP process and packaging equipment, utilities & facilities.Coordinate, develop and prepare installation, operation and performance qualification protocols for production equipment and production related facilities validation.Incl

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Contract, Third Party

Depends on Experience

Manager, Computer System Validation

Petersburg, Virginia

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Today

About Civica: Critical shortages of essential generic injectable drugs are an ongoing crisis in U.S. healthcare and have reached an all-time high. Over 300 essential medications are currently reported to be in shortage, according to industry and FDA reports. Shortages put patients at risk and waste hospital resources. Civica is a market-based nonprofit solution created in 2018 by health systems and philanthropies for the express purpose of preventing and mitigating drug shortages. Today, near

Full-time

CSV Engineer

Hybrid in Raritan, New Jersey

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13d ago

Job Description: Experience in validating ERP/SAP/ MES Manufacturing applications 3+ years experience with System Development Lifecyle 7+ years experience in Computer System Validation (Based on the role selected) Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation. Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation Experience in writing and executing docum

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Contract

Depends on Experience

Computer System Validation Engineer

Bothell, Washington

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Today

Job Title: Computer System Validation Engineer Location: Bothell, WA (50% Onsite) Duration: 6 Months Work Type: Hybrid (3 days a week onsite) and required to be onsite throughout UAT execution PURPOSE AND SCOPE OF POSITION: The Computer Systems Validation (CSV) Contractor works cross-functionally to lead and execute validation activities for GxP electronic systems and applications.This role is an individual contributor. The CSV Contractor will partner with Business Owners, Technical Owners, a

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Contract

$73 - $75

Computer System Validation Engineer 1

Remote

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Today

Title: CSV Engineer 1 Location: Remote About: The CSV Engineer 1 will support Computer System Validation (CSV) activities for GxP-regulated systems. This role involves executing validation deliverables, ensuring compliance with FDA 21 CFR Part 11, EU Annex 11, and company quality standards. The candidate will work closely with IT, Quality, and Business teams to maintain a validated state of systems. Key Responsibilities Assist in the development and execution of validation documentation, inclu

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Contract

Business Analyst

St. Louis, Missouri

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Today

RESPONSIBILITIES: Kforce has a client in Saint Louis, MO that is seeking a Business Analyst. Responsibilities: * Work with the Commercial Intelligence team to create and maintain BI tools that support Field Sales teams and Commercial leadership * Meet with stakeholders to gather and document requirements for new BI tools, communicate timelines and status updates, and ensure deliverables meet expectations * Combine data from various sources (Databricks, Excel, CSV, etc.) into a single data mode

Contract

$23 - $27 hourly

Fire Alarm System Programmer - Remote

Rocky Hill, Connecticut

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Today

Job DescriptionRemote PositionUnleash your potential with the Johnson Controls team! As a global leader in smart, healthy, and sustainable buildings, our mission is to reimagine the performance of buildings to serve people, places, and the planet. Join our winning team and pave the way for a bright future. With our extensive reach across various industries worldwide, our teams are uniquely positioned to support and empower you. You will have the opportunity to develop yourself through meaningful

Full-time

2026 Summer Internship Program: Engineering Validation Intern - Operational Technology and Computerized Systems Validation

Brooklyn Park, Minnesota

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Today

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description At Takeda's Brooklyn Park, MN, Facility, we manufacture Entyvio and Adcetris - monoclonal antibody therapies that help patients live

Full-time

USD 21.00 - 46.00 per hour

Computer System Validation Analyst

Foster City, California

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Today

Summary : Plan, lead, and execute the validation efforts for SCADA, Rockwell Factory Talk, PLC's and Ignition Create/write validation documentation (VP/URS/FS/DS/Trace Matrix/Risk Assessment/IQ/OQ/PQ, etc.) for process control systems. Author documents related to GxP Systems Draft Requirements and computer systems validation documents using GAMP 5 Execute test protocols for the software validation. Initiate and execute change management for existing qualified systems. Develop change management

Full-time

Computer System Validation Engineer

Princeton, New Jersey

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Today

Job Description Summary: The CSV Specialist is responsible for planning, coordinating, and executing validation activities for computer systems to ensure compliance with regulatory requirements. This role involves working closely with IT, Quality Assurance, and business stakeholders to validate new and existing systems, document validation evidence, and support audits and inspections. Roles & responsibility: Knowledge on FDA Guidance's and industry Standards Develop and execute validation plan

Full-time

Associate Director, Site Data Integrity and Computer System Validation Lead

Pleasant Prairie, Wisconsin

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Today

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined

Full-time

USD 111,000.00 - 178,200.00 per year

CSV Engineer

Wilson, North Carolina

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Today

Summary : We're looking for dedicated, innovative and driven talent to join our expanding team as we are currently looking to hire an CSV Engineer to join our projects team in Wilson, NC supporting multiple projects with the world's leading Pharmaceutical and Biotech company. Roles & Responsibilities: Automation Change Review and Approval Experience with Emerson Delta other DCS System Develop and complete continuous improvements as part of the validation team- Co-ordination of changes to ens

Full-time

Validation Engineer

Buffalo Grove, Illinois

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Today

Job Description: Strong knowledge of ERP systems. (implementations/validation). Expert writing test scripts, test functionality, data flow, documentation. CSV-Computer systems validation. Requirement management exp. (supporting planning for requirements, integrating requirements and the organization for working with them). Has worked in the manufacturing/med device space.

Full-time

Data Architect

Hybrid in Trenton, New Jersey

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8d ago

Job Description Position: Data Architect Location: Trenton, NJ, 08625 - (3 days on site, 2 days remote) Duration: 6 months contract Job Description We are in need of a Data Architect to research, design, develop, and evaluate data that support the creation of reports and dashboards which will be utilized for analytics. This would include the use of visualization tools, artificial intelligence, and machine learning. The Data Architect will work with Power BI and Python and have a strong understan

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Contract

Depends on Experience

CSV Engineer

Costa Mesa, California

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Today

Roles & Responsibilities: Bachelor's degree in engineering, Computer Science, Life Sciences, or related field. 2-10+ years of experience in computerized systems validation within pharmaceutical, biotechnology, or life sciences industries. Direct experience with GxP equipment, IT systems, or manufacturing automation systems. FDA and cGMP regulations and documentation practices. GAMP 5 guidance. 21 CFR Part 11 and Annex 11. Computer system validation methodologies. Familiarity with risk-based

Full-time

Automation Area Lead DeltaV

Hybrid in Indianapolis, Indiana

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Today

Automation Area Lead DeltaV Indiana, IN (Hybrid) Minimum 1 week a month in Indiana during the basic/detailed design phase of the project. Full-time on-site during the Commissioning phase of the project Project-based role, Duration 3 years The Automation Area Lead will be responsible for the control system solution for an area within a project, ensuring the solution is aligned with the overall program automation philosophy, standards, and user requirements. The area lead will work in conjunction

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Contract, Third Party

Depends on Experience

Senior CQV Engineer

Thousand Oaks, California

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Today

Job Summary : The Senior CQV Engineer will play a critical role in the successful startup and qualification of a new early-phase clinical biomanufacturing facility, encompassing cleanrooms, utilities, and a wide range of systems and equipment. This position is responsible for planning, executing, and documenting commissioning, qualification, and validation (CQV) activities to ensure all systems meet stringent regulatory and client-specific requirements Roles & Responsibilities: uthoring, editin

Full-time

IT CSV & CQV Validation Lead

Boston, Massachusetts

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Today

Responsibilities: Documentation & Deliverables: Develop and author comprehensive validation and quality documentation, including protocols, reports, risk assessments, SOPs, and other project-related materials. Ensure all documentation complies with applicable regulatory standards such as FDA, EMA, GxP, and other relevant guidelines. Review and approve validation documents to confirm alignment with both project objectives and regulatory requirements. Project Management: Lead and oversee multiple

Full-time

Jasper Developer

Weehawken Township, New Jersey

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6d ago

Job Title: Jasper Developer Location: Weehawken, NJ Duration: 6 Months Contract to Hire Interview: Virtual Job Descriptions: 7+ years of experience as a Jasper developer. Senior Jasper Reports Developer. Must be able to design complex reports using Jaspersoft Studio. Knowledge of report deployment and configuration is a must. Knowledge of Jaspersoft Architecture and Deployment. Design, develop, and support reports using the Jaspersoft reporting platform and related tools. Experience in develo

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Full-time, Part-time, Third Party, Contract

Validation Engineer

Birmingham, Alabama

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Today

Responsibilities: Develop URS, SIC and SRA for new and existing aseptic facilities and equipment. Develop and execute Commissioning (COM) and Installation qualification (IQ) protocols to ensure that systems are installed correctly and according to specifications. Perform operational qualification (OQ) and performance qualification (PQ) activities to verify that systems operate as intended under all conditions. Ensure all documentation is compliant with regulatory requirements and internal qualit

Full-time

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Computerized System Validation jobs in MO